Prematurity, RoP & NEC Flashcards

1
Q

Define premature birth

A

<37 weeks gestation

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2
Q

Define:

1) extreme preterm

2) very preterm

3) moderate to late preterm

A

1) before 28 weeks

2) 28-32 weeks

3) 32 to 37 weeks

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3
Q

What are some identified risk factors for premature delivery?

A

1) Previous preterm delivery

2) Multiple pregnancy

3) Smoking and illicit drug use in pregnancy

4) Being over or underweight in pregnancy

5) Early pregnancy (within 6 months of previous pregnancy)

6) Problems involving cervix, uterus or placenta:
- infection
- eclampsia
- placental abruption

7) Premature or prelabour rupture of membranes

8) Maternal comorbidities such as diabetes and hypertension

9) Physical injury/trauma

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4
Q

In women with a history of preterm birth or an US demonstrating a cervical length of 25mm or less before 24 weeks gestation, what are the two options of trying to delay birth?

A

1) Prophylactic vaginal progesterone –> putting a progesterone suppository in the vagina to discourage labour

2) Prophylactic cervical cerclage –> putting a suture in the cervix to hold it closed

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5
Q

Where preterm labour is suspected or confirmed, what are the options for improving the outcomes?

A

1) Tocolysis with nifedipine

2) Maternal corticosteroids

3) IV Magnesium sulphate

4) Delayed cord clamping or cord milking

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6
Q

What class of drug is nifedipine?

A

A calcium channel blocker

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7
Q

What is the role of nifedipine in premature labour?

A

Tocolysis –> Nifedipine is a calcium channel blocker that suppresses labour

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8
Q

Define tocolysis

A

Tocolytics are medications used to suppress premature labor.

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9
Q

When should maternal steroids be given in premature delivery?

A

If between 26-34 weeks gestation

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10
Q

Role of steroids in preterm labour?

A

Reduce incidence of respiratory distress syndrome by stimulating development of lungs.

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11
Q

Role of IV Magnesium sulphate in preterm delivery?

A

Neuroprotective for baby

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12
Q

Role of delayed cord clamping or cord milking in preterm?

A

Can increase the circulating blood volume and haemoglobin in the baby

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13
Q

What issues in early life can prematurity lead to?

A

1) RDS

2) Hypothermia

3) Hypoglycaemia

4) Poor feeding

5) Apnoea and bradycardia

6) Neonatal jaundice

7) Intraventricular haemorrhage

8) Retinopathy of prematurity

9) Necrotising enterocolitis

10) Immature immune system and infection

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14
Q

What long term effects can prematurity have?

A

1) Chronic lung disease of prematurity (CLDP)

2) Learning and behavioural difficulties

3) Susceptibility to infections, particularly respiratory tract infections

4) Hearing and visual impairment

5) Cerebral palsy

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15
Q

At what gestation age should resuscitation not be performed in premature babies?

A

<23 weeks

Between 23 and 23+6 weeks then there may be a decision not to start resuscitation in the best interests of the baby, especially if parents have expressed this wish.

Between 24 and 24+6 weeks, resuscitation should be commenced unless the baby is thought to be severely compromised

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16
Q

At what gestation age is it appropriate to resuscitate and start intensive care?

A

After 25 weks

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17
Q

What respiratory complications may be caused by prematurity?

A

1) Respiratory distress syndrome

2) Surfactant deficient lung disease

3) Chronic lung disease/ Bronchopulmonary dysplasia

4) Recurrent apnoea

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18
Q

What is retinopathy of prematurity RoP)?

A

A condition affecting preterm and low birth weight babies.

It is a potentially blinding condition caused by the abnormal development of the blood vessels in the retina can lead to scarring, retinal detachment and blindness.

Treatment can prevent blindness, which is why screening is so important.

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19
Q

What age gestation does RoP typically present?

A

Babies born <32 weeks gestation

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20
Q

At what gestational age does retinal blood vessel development start?

A

Around 16 weeks, is complete by 37 – 40 weeks gestation.

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21
Q

What is retinal blood vessel development stimulated by?

A

Hypoxia (which is a normal condition in the retina during pregnancy).

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22
Q

How does prematurity cause RoP?

A

1) When the retina is exposed to higher oxygen concentrations in a preterm baby, particularly with supplementary oxygen during medical care, the stimulant for normal blood vessel development is removed.

2) When the hypoxic environment recurs, the retina responds by producing excessive blood vessels (neovascularisation), as well as scar tissue.

3) These abnormal blood vessels may regress and leave the retina without a blood supply.

4) The scar tissue may cause retinal detachment.

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23
Q

What are the 3 key risk factors for RoP?

A

1) Prematurity (<32 weeks gestation).

2) Low birthweight (<1500g, significantly increased if <1250g).

3) Uncontrolled hyper-oxygenation (previously common practice to give high-flow oxygen to premature infants to ensure adequate oxygenation however this was shown to cause ischaemic effects in retinal development and is considered the first stage in the development of ROP).

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24
Q

How can high flow oxygen in premature infants cause RoP?

A

This was shown to cause ischaemic effects in retinal development and is considered the first stage in the development of ROP.

Over oxygenation (e.g. during ventilation) results in a proliferation of retinal blood vessels (neovascularisation).

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25
Q

What 3 zones is the retina divided into?

A

Zone 1 includes the optic nerve and the macula.

Zone 2 is from the edge of zone 1 to the ora serrata, the pigmented border between the retina and ciliary body.

Zone 3 is outside the ora serrata.

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26
Q

How is RoP staged?

A

The areas of disease are described from stage 1 (slightly abnormal vessel growth) to stage 5 (complete retinal detachment).

“Plus disease” describes additional findings, such as tortuous vessels and hazy vitreous humour.

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27
Q

Under what circumstances would babies be screened for RoP?

A

1) Infants born <31 weeks gestational age

OR

2) Infants born <1.5kg birth weight

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28
Q

How long should RoP screening continue for?

A

Screening should happen at least every 2 weeks and can cease once the retinal vessels enter zone 3, usually at around 36 weeks gestation.

29
Q

What are the 2 mainstays of management of RoP?

A

1) Transpupillary laser photocoagulation

2) Anti-VEGF

30
Q

Role of laser therapy in the management of RoP?

A

Successfully reverses ROP in 90% cases.

Involves use of laser to “burn” abnormal areas of the retina in which there is inadequate vascularisation.

This burning process prevents abnormal blood vessel proliferation.

31
Q

Role of anti-VEGF in RoP?

A

In some cases in which either laser-therapy has been unsuccessful and/or the ophthalmologist deems it an appropriate early treatment option, the eye receives an injection of anti-VEGF solution.

This blocks the action of VEGF and effectively stops ongoing abnormal proliferation.

32
Q

What are the 3 key complications of RoP?

A

1) Infection

2) Cataracts

3) Retinal detachment

Children who are diagnosed with ROP are more likely to be short-sighted and develop a squint.

33
Q

What is the most common surgical emergency in neonates?

A

Necrotising enterocolitis (NEC)

34
Q

What is NEC?

A

Death (necrotising) of intestinal tissue (entero-) due to inflammation (colitis). This can lead to bowel perforation, peritonitis and shock.

It is a life threatening emergency that predominantly affects preterm infants.

35
Q

What are the 2 key risk factors for NEC?

A

1) Premature (especially <32 weeks)

2) Low birth weight (<1500g)

36
Q

Risk factors for NEC?

A

1) Low birth weight

2) Premature

3) Abnormal dopplers (measuring blood flow from the placenta to baby)

4) Antibiotic treatment lasting longer than 10 days or multiple courses of antibiotics

6) Enteral feeding

7) Use of cow’s milk formula (breastfeeding is protective against NEC)

8) Congenital heart disease

9) Respiratory distress and assisted ventilation

10) Sepsis

37
Q

What does the classic presentation of NEC include?

A

1) a new feeding intolerance

2) vomiting (may be bile or blood-stained)

3) abdo distension

4) haematochezia

5) if progresses: abdominal tenderness, abdominal oedema, erythema and palpable bowel loops (due to loop dilation)

6) systemic symptoms: apnoea, lethargy, bradycardia and decreased peripheral perfusion

38
Q

Exam findings in NEC?

A

1) Shiny distended abdomen, tender to palpation and can feel tense or “wooden”

2) Periumbilical erythema

3) Abdominal tenderness

4) Bilious gastric aspirate

5) Shock

6) Reduced bowel sounds

39
Q

What are 4 key differentials for NEC?

A

1) Sepsis

2) Intussusception

3) Volvulus

4) Hirschsprung’s disease

40
Q

What is Hirschsprung’s disease?

A

Caused by an aganglionic segment of bowel due to a developmental failure of the parasympathetic Auerbach and Meissner plexuses.

Although rare (occurring in 1 in 5,000 births) it is an important differential diagnosis in childhood constipation.

41
Q

What are the key presenting features of Hirschsprung’s disease?

A

Neonates –> failure or delay to pass meconium

Older children –> constipation, abdo distension

42
Q

What gestational age does NEC tend to occur?

A

Corrected gestational age of 30-33 weeks

43
Q

What is the diagnostic investigation for NEC?

A

AXR

44
Q

AXR features in NEC?

A

1) distended bowel loops

2) thickened bowel wall (bowel oedema)

3) intramural gas (pneumatosis intestinalis)

4) gas in the portal vein

5) pneumoperitoneum: in the later stages due to bowel perforation

45
Q

Lab investigations in NEC?

A

1) FBC: thrombocytopenia and neutropenia

2) CRP

3) ABG: metabolic acidosis or raised lactate

4) Blood culture: for sepsis

46
Q

If the bowel has perforated, Rigler’s sign may be visible.

What is this?

A

This occurs when both sides of the bowel wall are visible due to the presence of gas inside the lumen and within the peritoneal cavity.

47
Q

Key principles of MEDICAL management of NEC?

A

1) Nil by mouth (total parenteral nutrition may be required)

2) Bowel decompression with NG tube

3) Assess and manage sepsis

4) IV fluid resuscitation

5) IV Abx (broad-spectrum cover is recommended as first-line, such as cefotaxime and metronidazole)

6) Circulatory support and ventilation may be required

48
Q

Surgical management is required in what % of NEC cases?

A

20-50%

49
Q

What is the main indication for surgical intervention in NEC?

A

Evidence of perforation

50
Q

Surgical management of NEC?

A

A laparotomy is carried out to remove the perforated and necrotic bowel from the abdomen.

51
Q

What criteria is used to stage NEC?

A

Bell’s staging criteria

52
Q

Bell’s staging criteria for NEC:

A

Stage I: suspected NEC

Stage II: proven NEC

Stage III: advanced NEC

53
Q

What indicates stage I NEC?

A

Signs –> Lethargy, apnoea, temperature instability, abdominal distention, vomiting, heme-positive stool

AXR –> Radiology may be normal or show intestinal dilation

54
Q

What indicates stage II NEC?

A

Signs –> Similar to stage I with abdominal tenderness, abdominal wall discolouration, abdominal mass, mild metabolic acidosis

AXR –> Intestinal dilation, ileus, ascites, pneumatosis intestinalis

55
Q

What indicates stage III NEC?

A

Signs –> Critically ill neonate with hypotension, bradycardia, peritonitis, respiratory and metabolic acidosis, disseminated intravascular coagulation

AXR –> Pneumoperitoneum

56
Q

General complications of NEC?

A

1) Bowel perforation

2) DIC

3) Sepsis

4) Adverse neurodevelopmental outcomes (especially in infants who undergo surgery)

5) Long term stoma

57
Q

Post-op complications of NEC?

A

1) Short bowel syndrome

2) Formation of intestinal strictures

3) Enterocolic fistulae

4) Abscess formation

5) Death –> In infants who undergo surgery for NEC, a 29% post-surgical mortality rate has been reported at one year.

58
Q

What will U&Es show in NEC?

A

Hyponatraemia

59
Q

Define apnoea

A

Periods where breathing stops spontaneously for more than 20 seconds, or shorter periods with oxygen desaturation or bradycardia.

60
Q

What is the key risk factor for apnoea in neonates?

A

Prematurity.

They occur in almost all babies <28 weeks gestation and the incidence decreases with increased gestational age.

In term infants apnoea usually indicate underlying pathology.

61
Q

What does apnoea indicate in preterm vs term neonates

A

Preterm –> very common

Term –> usually indicates underlying pathology.

62
Q

What causes apnoea?

A

Apnoea occur due to immaturity of the autonomic nervous system that controls respiration and heart rate. This system is more immature in premature neonates.

63
Q

Apnoea are often a sign of developing illness, such as…?

A

1) Infection

2) Anaemia

3) Airway obstruction (may be positional)

4) CNS pathology, such as seizures or haemorrhage

5) Gastro-oesophageal reflux

6) Neonatal abstinence syndrome

64
Q

Management of apnoea of prematurity?

A

1) Neonatal units attach apnoea monitors to premature babies –> these make a sound when an apnoea is occurring.

2) Tactile stimulation is used to prompt the baby to restart breathing.

3) IV caffeine can be used to prevent apnoea and bradycardia in babies with recurrent episodes.

65
Q

Prognosis of apnoea of prematurity?

A

Episodes will settle as as the baby grows and develops.

66
Q

What is used to prompt the baby to restart breathing in apnoea or prematurity?

A

Tactile stimulation

67
Q

What can be used to prevent apnoea and bradycardia in babies with recurrent episodes of apnoea of prematurity?

A

IV caffeine

68
Q
A